2gtg

Disease
Known disease associated with this structure: Combined SAP deficiency OMIM:[176801], Gaucher disease, atypical OMIM:[176801], Krabbe disease, atypical OMIM:[176801], Metachromatic leukodystrophy due to SAP-b deficiency OMIM:[176801]

About this Structure
2GTG is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference
Page seeded by OCA on Mon Feb 16 20:47:05 2009